TMIE Antikörper (Middle Region)

Produktnummer ABIN955258

Produktdetails anti-TMIE Antikörper

Target: TMIE (Transmembrane Inner Ear (TMIE))

Bindungsspezifität: AA 78-108, Middle Region

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser TMIE Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Enzyme Immunoassay (EIA)

Spezifität: This antibody detects TMIE (Center).

Kreuzreaktivität (Details): Species reactivity (tested):Human

Aufreinigung: Protein A column followed by peptide affinity purification

Immunogen: KLH conjugated synthetic peptide between 78~108 amino acids from the Central region of human TMIE

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: Optimal working dilution should be determined by the investigator.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.25 mg/mL

Buffer: PBS with 0.09 % (W/V) sodium azide

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Handhabung: Avoid repeated freezing and thawing.

Lagerung: 4 °C/-20 °C

Informationen zur Lagerung: Store at 2 - 8 °C for up to six months or (in aliquots) at -20 °C for longer.

Details zu TMIE

Target: TMIE (Transmembrane Inner Ear (TMIE))

Andere Bezeichnung: TMIE (TMIE Produkte)

Synonyme: si:ch211-163f10.1 antikoerper, DFNB6 antikoerper, 5131400L21Rik antikoerper, Mm.87012 antikoerper, sr antikoerper, RGD1562523 antikoerper, transmembrane inner ear antikoerper, tmie antikoerper, TMIE antikoerper, Tmie antikoerper

Hintergrund: This gene encodes a transmembrane inner ear protein. Studies in mouse suggest that this gene is required for normal postnatal maturation of sensory hair cells in the cochlea, including correct development of stereocilia bundles. This gene is one of multiple genes responsible for recessive non-syndromic deafness (DFNB), also known as autosomal recessive nonsyndromic hearing loss (ARNSHL), the most common form of congenitally acquired inherited hearing impairment.Synonyms: Transmembrane inner ear expressed protein

Gen-ID: 259236

NCBI Accession: NP_671729

Pathways: Sensory Perception of Sound